THBS1 is a new autosomal recessive non-syndromic hearing impairment gene

Bharadwaj, T., Acharya, A., Khan, F. U., Khan, S., Ullah, I., Schrauwen, I., Ahmad, W., & Leal, S. M. (2024). THBS1 is a new autosomal recessive non-syndromic hearing impairment gene. BMC Medical Genomics, 17(1). https://doi.org/10.1186/s12920-024-02060-w
Authors:
Thashi Bharadwaj
Anushree Acharya
Fati Ullah Khan
Saadullah Khan
Irfan Ullah
Isabelle Schrauwen
Wasim Ahmad
Suzanne M. Leal
Affiliated Authors:
Thashi Bharadwaj
Anushree Acharya
Suzanne M. Leal
Columbia Affiliation:
Subjects:
Thrombospondin 1 (MeSH)
Pedigree (MeSH)
Genes, Recessive (MeSH)
Cochlear Neuropathy and Hearing Loss Mechanisms (OpenAlex Topic)
Role of Long Noncoding RNAs in Cancer and Development (OpenAlex Topic)
Molecular Mechanisms of Cardiac Development and Regeneration (OpenAlex Topic)
Author Keywords:
autosomal recessive non-syndromic hearing impairment
consanguinity
exome sequencing
inner ear
thrombospondin
thbs1
elink
Publication Type:
Article
Unique ID:
10.1186/s12920-024-02060-w
PMID:
39696404
DOI:
10.1186/s12920-024-02060-w
Journal:
BMC Medical Genomics
Publication Date:
Data Source:
OpenAlex
Source Link:
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